Page 1 of Clinical Trials for "Mitochondrial Diseases", 81 Total Matches
- 1TerminatedLast Updated: September 12, 2011Condition(s): Mitochondrial Disease
- 2TerminatedLast Updated: August 4, 2005Condition(s): Mitochondrial Diseases
- 3RecruitingLast Updated: March 19, 2012Condition(s): Mitochondrial Diseases
- 4CompletedLast Updated: February 24, 2012Condition(s): Gastrointestinal Dysfunction; Mitochondrial Disorders
- 5RecruitingLast Updated: June 9, 2011Condition(s): Mitochondrial Diseases
- 6CompletedLast Updated: February 3, 2012Condition(s): MELAS Syndrome; Mitochondrial Diseases
- 7RecruitingLast Updated: January 28, 2009Condition(s): Mitochondrial Diseases; Diagnosis; DNA Mutations
- 8RecruitingLast Updated: September 20, 2011Condition(s): Gulf War Syndrome; Mitochondrial Disease
- 9CompletedLast Updated: April 27, 2012Condition(s): Mitochondrial Disease
- 10Enrolling by invitationLast Updated: October 28, 2011Condition(s): Mitochondrial Disease
- 11RecruitingLast Updated: April 13, 2011Condition(s): Mitochondrial Disease
- 12RecruitingLast Updated: February 14, 2012Condition(s): Mitochondrial DNA Mutation
- 13CompletedLast Updated: October 28, 2011Condition(s): Metabolic Syndrome; Type 2 Diabetes Mellitus
- 14Not yet recruitingLast Updated: November 23, 2011Condition(s): Chronic Fatigue Syndrome
- 15Active, not recruitingLast Updated: June 23, 2005Condition(s): MELAS Syndrome
- 16CompletedLast Updated: January 13, 2009Condition(s): Mitochondrial Respiratory Chain Deficiencies
- 17CompletedLast Updated: December 15, 2011Condition(s): Very Long-chain Acyl-CoA Dehydrogenase Deficiency; Trifunctional Protein Deficiency; Carnitine Palmitoyltransferase 2 Deficiency; Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- 18RecruitingLast Updated: December 1, 2011Condition(s): Dyskeratosis Congenita; Fanconi Anemia; Myelodysplastic Syndromes; Nonmalignant Neoplasm; Pearson Marrow-pancreas Syndrome; Shwachman-diamond Syndrome
- 19Active, not recruitingLast Updated: July 20, 2011Condition(s): Carnitine Palmitoyltransferase II Deficiency; Very Long Chain Acyl Coa Dehydrogenase Deficiency
- 20CompletedLast Updated: June 24, 2010Condition(s): Pompe Disease (Late-onset); Glycogen Storage Disease Type II (GSD-II); Acid Maltase Deficiency Disease; Glycogenosis 2
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Mitochondrial+Diseases%22
